NeuralCipher Source record
LRRK2 pathobiology in Parkinson's disease.
DOI: 10.1111/jnc.12949PMID: 25251388
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
14.182 articles found
Open access
Rab11 modulates α-synuclein-mediated defects in synaptic transmission and behaviour.
DOI: 10.1093/hmg/ddu521PMID: 25305083
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access
Nutrient deprivation induces α-synuclein aggregation through endoplasmic reticulum stress response and SREBP2 pathway.
DOI: 10.3389/fnagi.2014.00268PMID: 25339898
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Should genetic testing for SCAs be included in the diagnostic workup for MSA?
DOI: 10.1212/wnl.0000000000000965PMID: 25298309
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
Open access
Formation of α-synuclein Lewy neurite-like aggregates in axons impedes the transport of distinct endosomes.
DOI: 10.1091/mbc.e14-02-0741PMID: 25298402
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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An exome study of Parkinson's disease in Sardinia, a Mediterranean genetic isolate.
DOI: 10.1007/s10048-014-0425-xPMID: 25294124
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Besides fibrillization: putative role of the peptide fragment 71-82 on the structural and assembly behavior of α-synuclein.
DOI: 10.1021/bi5008707PMID: 25255476
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Changes in actin dynamics and F-actin structure both in synaptoneurosomes of LRRK2(R1441G) mutant mice and in primary human fibroblasts of LRRK2(G2019S) mutation carriers.
DOI: 10.1016/j.neuroscience.2014.09.070PMID: 25301747
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Open access
Novel ethyl methanesulfonate (EMS)-induced null alleles of the Drosophila homolog of LRRK2 reveal a crucial role in endolysosomal functions and autophagy in vivo.
DOI: 10.1242/dmm.017020PMID: 25288684
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Cerebrospinal fluid alpha-synuclein as a biomarker for Parkinson's disease diagnosis: a systematic review and meta-analysis.
DOI: 10.3109/00207454.2014.961454PMID: 25202803
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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The complex relationships between microglia, alpha-synuclein, and LRRK2 in Parkinson's disease.
DOI: 10.1016/j.neuroscience.2014.09.049PMID: 25284317
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Heterogeneity of leucine-rich repeat kinase 2 mutations: genetics, mechanisms and therapeutic implications.
DOI: 10.1007/s13311-014-0284-zPMID: 24957201
A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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